Ricardo Gracía

735 total citations
17 papers, 461 citations indexed

About

Ricardo Gracía is a scholar working on Molecular Biology, Genetics and Endocrinology, Diabetes and Metabolism. According to data from OpenAlex, Ricardo Gracía has authored 17 papers receiving a total of 461 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 8 papers in Genetics and 6 papers in Endocrinology, Diabetes and Metabolism. Recurrent topics in Ricardo Gracía's work include Sexual Differentiation and Disorders (5 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers) and Hormonal and reproductive studies (3 papers). Ricardo Gracía is often cited by papers focused on Sexual Differentiation and Disorders (5 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers) and Hormonal and reproductive studies (3 papers). Ricardo Gracía collaborates with scholars based in Spain, Argentina and Australia. Ricardo Gracía's co-authors include Begoña Ezquieta, Karen E. Heath, Ángel Campos‐Barros, Sara Benito‐Sanz, Jesús Argente, Pablo Lapunzina, Miriam Aza‐Carmona, Vicente Barrios, Francisca Díaz and Antonio González‐Meneses and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, Journal of Medical Genetics and Human Genetics.

In The Last Decade

Ricardo Gracía

17 papers receiving 451 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Ricardo Gracía Spain 11 277 241 183 64 50 17 461
Celsa Quinteiro Spain 13 213 0.8× 160 0.7× 247 1.3× 26 0.4× 65 1.3× 20 521
Mariarosaria Lang‐Muritano Switzerland 14 366 1.3× 375 1.6× 337 1.8× 64 1.0× 176 3.5× 35 756
Esperanza Berensztein Argentina 14 316 1.1× 236 1.0× 168 0.9× 43 0.7× 116 2.3× 34 598
L Duprez Belgium 14 271 1.0× 190 0.8× 395 2.2× 106 1.7× 90 1.8× 16 656
Gabriela P. Finkielstain United States 13 671 2.4× 302 1.3× 503 2.7× 108 1.7× 53 1.1× 17 877
Mary M. Lee United States 8 260 0.9× 200 0.8× 67 0.4× 87 1.4× 59 1.2× 16 601
María Sonia Baquedano Argentina 11 244 0.9× 224 0.9× 200 1.1× 37 0.6× 55 1.1× 19 462
Abdulsalam Abu‐Libdeh Israel 10 187 0.7× 115 0.5× 75 0.4× 23 0.4× 66 1.3× 25 338
Jérôme Dulon France 14 385 1.4× 214 0.9× 271 1.5× 72 1.1× 22 0.4× 28 737
Nora Saraco Argentina 14 339 1.2× 383 1.6× 205 1.1× 62 1.0× 66 1.3× 25 661

Countries citing papers authored by Ricardo Gracía

Since Specialization
Citations

This map shows the geographic impact of Ricardo Gracía's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Ricardo Gracía with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ricardo Gracía more than expected).

Fields of papers citing papers by Ricardo Gracía

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ricardo Gracía. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Ricardo Gracía. The network helps show where Ricardo Gracía may publish in the future.

Co-authorship network of co-authors of Ricardo Gracía

This figure shows the co-authorship network connecting the top 25 collaborators of Ricardo Gracía. A scholar is included among the top collaborators of Ricardo Gracía based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Ricardo Gracía. Ricardo Gracía is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

17 of 17 papers shown
1.
Benito‐Sanz, Sara, José Luís Royo, Eva Barroso, et al.. (2012). Identification of the first recurrent PAR1 deletion in Léri-Weill dyschondrosteosis and idiopathic short stature reveals the presence of a novel SHOX enhancer. Journal of Medical Genetics. 49(7). 442–450. 55 indexed citations
2.
Aza‐Carmona, Miriam, Eva Barroso, Damián Heine‐Suñer, et al.. (2011). Identification of a Gypsy SHOX mutation (p.A170P) in Léri-Weill dyschondrosteosis and Langer mesomelic dysplasia. European Journal of Human Genetics. 19(12). 1218–1225. 8 indexed citations
3.
Benito‐Sanz, Sara, et al.. (2011). Identification of the first PAR1 deletion encompassing upstream SHOX enhancers in a family with idiopathic short stature. European Journal of Human Genetics. 20(1). 125–127. 39 indexed citations
4.
Aza‐Carmona, Miriam, et al.. (2011). Familial glucocorticoid deficiency due to compound heterozygosity of two novel MC2R mutations. Journal of Pediatric Endocrinology and Metabolism. 24(5-6). 395–7. 4 indexed citations
5.
Barroso, Eva, Sara Benito‐Sanz, Patricia Yuste‐Checa, et al.. (2010). Identification of the first de novo PAR1 deletion downstream of SHOX in an individual diagnosed with Léri–Weill dyschondrosteosis (LWD). European Journal of Medical Genetics. 53(4). 204–207. 6 indexed citations
6.
Martínez‐Glez, Víctor, Valeria Romanelli, María Ángeles Mori, et al.. (2010). Macrocephaly–capillary malformation: Analysis of 13 patients and review of the diagnostic criteria. American Journal of Medical Genetics Part A. 152A(12). 3101–3106. 38 indexed citations
7.
Solera, Jesús, Pedro Arias, I. González Casado, et al.. (2009). Identification of eight new mutations in the GCK gene by DHPLC screening in a Spanish population. Diabetes Research and Clinical Practice. 85(1). 20–23. 5 indexed citations
8.
Heath, Karen E., Jesús Argente, Vicente Barrios, et al.. (2008). Primary Acid-Labile Subunit Deficiency due to RecessiveIGFALSMutations Results in Postnatal Growth Deficit Associated with Low Circulating Insulin Growth Factor (IGF)-I, IGF Binding Protein-3 Levels, and Hyperinsulinemia. The Journal of Clinical Endocrinology & Metabolism. 93(5). 1616–1624. 54 indexed citations
9.
10.
Ortega‐Gutiérrez, Silvia, Alicia Delicado, María Ángeles Mori, et al.. (2006). The G397A (E133K) change in the AGGF1 (VG5Q) gene is a single nucleotide polymorphism in the Spanish population. American Journal of Medical Genetics Part A. 140A(24). 2832–2833. 9 indexed citations
11.
Gurrieri, Fiorella, Giovanni Neri, Antonio González‐Meneses, et al.. (2005). Clinical and molecular studies on two further families with Simpson‐Golabi‐Behmel syndrome. American Journal of Medical Genetics Part A. 138A(3). 272–277. 19 indexed citations
12.
Fernández‐Cancio, Mónica, Manuel Nistal, Ricardo Gracía, et al.. (2004). Compound Heterozygous Mutations in the SRD5A2 Gene Exon 4 in a Male Pseudohermaphrodite Patient of Chinese Origin. Journal of Andrology. 25(3). 412–416. 28 indexed citations
13.
Lassaletta, Luis, et al.. (1999). Intestinal lengthening and growth hormone in extreme short bowel syndrome: A case report. Journal of Pediatric Surgery. 34(9). 1423–1424. 18 indexed citations
14.
Ezquieta, Begoña, et al.. (1997). MICROSATELLITE MARKERS IN THE INDIRECT ANALYSIS OF THE STEROID 21-HYDROXYLASE GENE. Prenatal Diagnosis. 17(5). 429–434. 15 indexed citations
15.
Lapunzina, Pablo, Eduardo Fonseca, Ricardo Gracía, & Alicia Delicado. (1995). Rothmund‐Thomson Syndrome and Addison Disease. Pediatric Dermatology. 12(2). 164–169. 2 indexed citations
16.
Ezquieta, Begoña, et al.. (1995). Analysis of steroid 21-hydroxylase gene mutations in the Spanish population. Human Genetics. 96(2). 198–204. 105 indexed citations
17.
Lapunzina, Pablo, José Ignacio Rodrı́guez, Elena De Matteo, Ricardo Gracía, & Felipe Moreno. (1995). Mulibrey nanism: Three additional patients and a review of 39 patients. American Journal of Medical Genetics. 55(3). 349–355. 18 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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